Synthesis and Preliminary Evaluation of 9-(4-18FFluoro-3-hydroxymethylbutyl) Guanine (18FFHBG) in HSV1-tk Gene Transduced Hepatoma Cell.
- Author:
Byung Seok MOON
1
;
Tae Sup LEE
;
Myoung Keun LEE
;
Kyo Chul LEE
;
Gwang Il AN
;
Kwon Soo CHUN
;
Ok Doo AWH
;
Dae Yoon CHI
;
Chang Woon CHOI
;
Sang Moo LIM
;
Gi Jeong CHEON
Author Information
1. Laboratory of Radiopharmaceuticals, Korea Institute of Radiological and Medical Sciences, Seoul, Korea. larry@kcch.re.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
[18F]FHBG;
thymidine kinase;
gene therapy;
PET
- MeSH:
Animals;
Carcinoma, Hepatocellular*;
Cell Count;
Gene Expression;
Genes, Reporter;
Genetic Therapy;
Guanine*;
Mice;
Suicide;
Thymidine Kinase
- From:Nuclear Medicine and Molecular Imaging
2006;40(4):218-227
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: The HSV1-tk reporter gene system is the most widely used system because of its advantage that direct monitoring is possible without the introduction of a separate reporter gene in case of HSV1-tk suicide gene therapy. In this study, we investigate the usefulness of the reporter probe (substrate), 9-(4-[18F]fluoro-3-hydroxymethylbutyl)guanine ([18F]FHBG) for non-invasive reporter gene imaging using PET in HSV1-tk expressing hepatoma model. MATERIALS AND METHODS: Radiolabeled FHBG was prepared in 8 steps from a commercially available triester. The labeling reaction was carried out by NCA nucleophilic substitution with K[18F]/K2.2.2. in acetonitrile using N2-monomethoxytrityl-9-[4-(tosyl)-3-monomethoxytritylmethylbutyl]guanine as a precursor, followed by deprotection with 1 N HCl. Preliminary biological properties of the probe were evaluated with MCA cells and MCA-tk cells transduced with HSV1-tk reporter gene. In vitro uptake and release-out studies of [18F]FHBG were performed, and was analyzed correlation between [18F]FHBG uptake ratio according to increasing numeric count of MCA-tk cells and degree of gene expression. MicroPET scan image was obtained with MCA and MCA-tk tumor bearing Balb/c-nude mouse model. RESULTS: [18F]FHBG was purified by reverse phase semi-HPLC system and collected at around 16-18 min. Radiochemical yield was about 20-25% (corrected for decay), radiochemical purity was >95% and specific activity was around >55.5 GBq/micro mol. Specific accumulation of [18F]FHBG was observed in HSV1-tk gene transduced MCA-tk cells but not in MCA cells, and consecutive 1 hour release-out results showed more than 86% of uptaked [18F]FHBG was retained inside of cells. The uptake of [18F]FHBG was showed a highly significant linear correlation (R2=0.995) with increasing percentage of MCA-tk numeric cell count. In microPET scan images, remarkable difference of accumulation was observed for the two type of tumors. CONCLUSION: [18F]FHBG appears to be a useful as non-invasive PET imaging substrate in HSV1-tk expressing hepatoma model.
